Our services are flexible thanks to our Functional Service Provider (FSP Model)​ which works well for small and mid-sized Biotech with PIPELINE in development and CROs that need coverage in our region, that mainly have their own capabilities.
We provide tailor made solution for:

• Feasibility and Site selection;
• Regulatory and Ethics Committee Submission;
• Site Start-up activities;
• Safety Reporting;
• Site contracts execution and budget negotiation;
• Clinical monitoring;
• Site and Project management;
• Data management support;
• Quality management support;
• Investigator grant payment management;
• Import and Export License execution;
• Custom clearance clinical supply and equipment storage;
• Türkiye Legal representation (KVKK/Verbis)

All services are on demand. Our team is operating according to client SOPs within the FSP Model.​

Our Exprience is defined by more than two dozens Clinical Trials completed in the past 6 years.

See trials​

Founded in 2019, Rosenbaum Group has grown from an entrepreneurial vision into an operational team of over 20 professionals with experience across leading international CROs.
We specialize in navigating complex European regions, where operational expertise, local insight, and execution excellence make the difference between delay and delivery.
Our focus is clear: reliable outcomes, efficient patient recruitment, operational excellence, and a sustainable return on investment.
​

Why?

We know how important is to know Sites & Investigators when it comes to recruitment, quality and delivery.​

Through long‑standing professional relationships, we collaborate with a carefully selected group of investigators and site teams who share our commitment to quality and performance.
This close cooperation enables strong patient recruitment results, with enrollment goals often achieved on time. ​